Functions of the M-CSF receptor on osteoclasts
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Updated: Nov 2, 2026

Effect of Anti-c-fms Antibody on Osteoclast Formation and Proliferation of Osteoclast Precursor In Vitro
Published on: March 18, 2019
S Yang1, Y Zhang, R M Rodriguiz
1Department of Pediatrics, Medical University of South Carolina, Charleston, USA.
Abstract:
Macrophage colony-stimulating factor (M-CSF) receptor has been previously reported to be present in osteoclasts both at mRNA and protein levels. However, the biochemical interactions between M-CSF and its receptor on osteoclasts are less well characterized than in mononuclear phagocytes. In this study, we show that (1) 125I-labeled M-CSF ligand specifically binds to the M-CSF receptor on osteoclasts by autoradiography; (2) binding of M-CSF to the receptor stimulates protein tyrosine phosphorylation in osteoclasts by immunostaining; (3) oxygen-derived free radicals produced by calvarial osteoclasts are increased by M-CSF stimulation (1.37 +/- 0.08, n = 10, P < 0.01); and (4) bone resorption in calvarial explants is enhanced by M-CSF (1.153 +/- 0.09, n = 10, p < 0.001). Thus, our data provide multiple lines of evidences that mouse calvarial osteoclasts are activated by M-CSF. These data suggest that under the conditions present in the calvarial model, M-CSF activates osteoclastic bone resorption.
Insights
Macrophage colony-stimulating factor (M-CSF) activates osteoclasts, enhancing bone resorption. This study demonstrates M-CSF binding stimulates osteoclast activity and increases bone resorption in mouse calvarial explants.
Area of Science:
- Bone Biology
- Cell Signaling
- Osteoclast Biology
Background:
- Macrophage colony-stimulating factor (M-CSF) receptor is present in osteoclasts.
- Biochemical interactions between M-CSF and its receptor on osteoclasts are not fully understood.
Purpose of the Study:
- To investigate the biochemical interactions between M-CSF and its receptor on osteoclasts.
- To determine the effect of M-CSF on osteoclast function and bone resorption.
Main Methods:
- Autoradiography to assess M-CSF ligand binding to osteoclast receptors.
- Immunostaining to detect protein tyrosine phosphorylation.
- Measurement of oxygen-derived free radicals produced by osteoclasts.
- Assessment of bone resorption in calvarial explants.
Main Results:
- 125I-labeled M-CSF specifically binds to the M-CSF receptor on osteoclasts.
- M-CSF binding stimulates protein tyrosine phosphorylation in osteoclasts.
- M-CSF stimulation increases oxygen-derived free radical production by osteoclasts.
- M-CSF enhances bone resorption in calvarial explants.
Conclusions:
- Mouse calvarial osteoclasts are activated by M-CSF.
- M-CSF stimulates osteoclastic bone resorption.
- These findings suggest M-CSF plays a role in regulating bone resorption in the calvarial model.
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